🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Writer Login
Latest
Clinical Trials in the UK / NCT06943755
Recruiting Phase 2/3

Zanzalintinib Versus Everolimus in Participants With Locally Advanced or Metastatic Neuroendocrine Tumors

NCT06943755 · tracked via the Priya Life Science UK tracker
Sponsor
Exelixis
Phase
Phase 2/3
Started
2025-07-21
Last updated
2026-09-10

Condition(s) studied

Pancreatic Neuroendocrine Tumor (pNET)Extra-Pancreatic Neuroendocrine Tumor (epNET)

Investigational drug(s) / intervention(s)

ZanzalintinibEverolimus

Zanzalintinib: Administered as specified in the treatment arm.

Everolimus: Administered as specified in the treatment arm.

Study summary

The primary purpose of this study is to assess the effectiveness of zanzalintinib compared to everolimus in participants with previously treated, unresectable, locally advanced or metastatic neuroendocrine tumors.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Key Inclusion Criteria: * Histologically confirmed, locally advanced/unresectable or metastatic, well-differentiated Grade 1, 2, or 3 NETs of pancreatic origin or extra-pancreatic origin. * Allowed prior lines of therapy, based on the site of NET and functional status. * Documented radiographic disease progression per RECIST 1.1, as assessed by the Investigator based on imaging assessments (computed tomography \[CT\] or magnetic resonance imaging \[MRI\]) within 12 months before randomization. * Measurable disease according to RECIST 1.1 as determined by the Investigator. * Archival tumor tissue is required, if available. If archival tumor tissue is not available, a fresh biopsy may be submitted if it can be safely and feasibly obtained. Every attempt should be made to provide tumor tissue. Key Exclusion Criteria: * Histologically confirmed neuroendocrine carcinomas (including small cell lung cancer), medullary thyroid cancer, pheochromocytoma, paraganglioma, Merkel cell carcinoma, and mixed neuroendocrine non-neuroendocrine neoplasm (MiNEN). * Prior treatment with a vascular endothelial growth factor receptor (VEGFR) -targeting tyrosine kinase inhibitor or a mammalian target of rapamycin (mTOR) inhibitor. * Systemic chemotherapy and any liver-directed or other ablative therapy within 4 weeks before randomization. * Systemic radionuclide therapy within 6 weeks before randomization. * Radiation therapy for bone metastases within 2 weeks, any other radiation therapy, except as indicated above, within 4 weeks before randomization. Note: Other protocol defined Inclusion/Exclusion criteria may apply.

Primary outcome measure(s)

Trial sites (126)

FacilityCityRegionStatus
The University of Alabama at Birmingham Birmingham Alabama Recruiting
Mayo Clinic Hospital Phoenix Arizona Recruiting
The University of Arizona Cancer Center Tucson Arizona Recruiting
Cedars-Sinai Medical Center Beverly Hills California Recruiting
Norris Comprehensive Cancer Center Los Angeles California Recruiting
Stanford Cancer Center Palo Alto California Recruiting
UCLA Health - Santa Monica Cancer Care Santa Monica California Recruiting
Kaiser Permanente Medical Center Vallejo California Recruiting
Georgetown University Washington D.C. District of Columbia Recruiting
Mayo Clinic - Florida Jacksonville Florida Recruiting
AdventHealth Orlando Orlando Florida Recruiting
Moffitt Cancer Center Tampa Florida Recruiting
University of Kentucky Markey Cancer Center Lexington Kentucky Recruiting
East Jefferson General Hospital Metairie Louisiana Recruiting
Dana-Farber Cancer Institute Boston Massachusetts Recruiting
Henry Ford Cancer- Detroit Detroit Michigan Recruiting
The Cancer and Hematology Centers Grand Rapids Michigan Recruiting
Mayo Clinic Rochester Minnesota Recruiting
Siteman Cancer Center St Louis Missouri Recruiting
University of Nebraska Medical Center Omaha Nebraska Recruiting
University of New Mexico Comprehensive Cancer Center Albuquerque New Mexico Recruiting
Roswell Park Cancer Institute Buffalo New York Recruiting
Icahan School of Medicine at Mount Sinai New York New York Recruiting
University of Rochester Medical Center Rochester New York Recruiting
University of North Carolina at Chapel Hill Chapel Hill North Carolina Recruiting
Duke University Medical Center Durham North Carolina Recruiting
Sanford Roger Maris Cancer Center Fargo North Dakota Recruiting
University Hospitals Cleveland Medical Center Cleveland Ohio Recruiting
The Ohio State University Comprehensive Cancer Center Columbus Ohio Recruiting
Oregon Health and Science University Portland Oregon Recruiting
University of Pennsylvania Philadelphia Pennsylvania Recruiting
University of Pittsburgh Medical Center (UPMC) Hillman Cancer Center Pittsburgh Pennsylvania Recruiting
University of Tennessee Medical Center Knoxville Tennessee Recruiting
Henry-Joyce Cancer Clinic Nashville Tennessee Recruiting
Texas Oncology- Baylor Charles A. Sammons Cancer Center Dallas Texas Recruiting
Huntsman Cancer Institute, University of Utah Salt Lake City Utah Recruiting
University of Virginia Charlottesville Virginia Recruiting
Virginia Cancer Specialists - Fairfax Office Fairfax Virginia Recruiting
Fred Hutchinson Cancer Center Seattle Washington Recruiting
Froedtert Hospital and the Medical College of Wisconsin Milwaukee Wisconsin Recruiting

+ 86 more sites — see the full list on the official registry below.

More Exelixis trials in the UK

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06943755 on ClinicalTrials.gov ↗ ← All trials in the UK